ZMP
elf3
Ensembl ID:
ZFIN ID:
Human Orthologue:
ELF3
Human Description:
E74-like factor 3 (ets domain transcription factor, epithelial-specific ) [Source:HGNC Symbol;Acc:33
Mouse Orthologue:
Elf3
Mouse Description:
E74-like factor 3 Gene [Source:MGI Symbol;Acc:MGI:1101781]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12768 | Essential Splice Site | Available for shipment | Available now |
sa18016 | Essential Splice Site | Available for shipment | Available now |
sa25170 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa24046 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12768
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113795 | Essential Splice Site | 123 | 375 | 3 | 8 |
Genomic Location (Zv9):
Chromosome 22 (position 638018)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 625126 |
GRCz11 | 22 | 662849 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCTGAKTTTTGGWGGCTGCATGCATTAACAATCTTTTTGTTGCATCCCT[A/G]GTTAATGACCTRTCTGAGAACACCGTCCTGRGCGAATCCGAGTTTGAGCT
Long Flanking Sequence:
CTTTGCGCAACATCCAAGGAAGCGCTGATGAGCATGTTCGGGCCGGAGTTGGGCAATCTGCTACACCACAGTCTGGAGAGCCTGAAGGCGAGATATGGTGAGTAACTGTTGTAGATAAACTTGCTGTTTAGTAATTGATGTTGAACTATTTGGAAGTAACACACACCTGAGGTGCTGATGTGGCCGTTAAACCTCATGATTTACTAAGAATTCAATGCCCTGGAATCAATGTAAAAGCATCTGTTAGGGATTCATTGTTTTGTCCTTAATCATCTCCTGTGTGTAGCACTAGTGTCCTCCACATCTCCTCCTGCTGCTGTGTTTTGTTGTGATTTTTGACTGTGGTAGTTGTGATTGAACTCATTCAGCGGGGTGATATGCAGCTGTAATGCACTCTTGAACTACTTCAGCTTTGAATTTATCCACAAACGCTCTTAAGGATGTAAACTGTTCTGATTTTTGGTGGCTGCATGCATTAACAATCTTTTTGTTGCATCCCT[A/G]GTTAATGACCTATCTGAGAACACCGTCCTGAGCGAATCCGAGTTTGAGCTACTAGACAACATCCTGCAGAACTCATTTCCCTCCATGCATGGACCAGGCCTGGGGCCTCTGCTGGAAACTGTGGTGGTCCAGTCTACAATTCCAACAGGTGAGCCGCAAATCCCACTCAAGACAAAAAACCCCCAGAGAGCAGGTCTATCCCTACTGGGAGTAACATTTAAAATTGTTTGTTGCAGACAATTCAGACGCCAAATACAGCTACTTCGATGAGTACACCAGCCAGCTGACCCCAGAGAGTGACCACGGCTACGACTCTCTCACGGAGAGCTTTCAGAGTTCCCATGCTGGTAAGAATCCCCACTAAAACCTAAACAACTCAGGTCAAGGGCGCTCTGTGAACGAACATTATTGAACATGTACTTCGGTTTGTCCTGTGTAGGCAGCTTCCTGAACCCGAGCTCACCTGAGTCCAACAGCAGTGATTCTGACCCTGAATACTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18016
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113795 | Essential Splice Site | 209 | 375 | 5 | 8 |
Genomic Location (Zv9):
Chromosome 22 (position 638456)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 625564 |
GRCz11 | 22 | 663287 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
RCGCTCTGTGAACGAACATTAYTGAACATGTRCTTYGGTTTGTCCTGTGT[A/C]GGCAGCTTCCTGAACCCGAGCTCACCTGAGTCCAACAGCAGTGATTCTGA
Long Flanking Sequence:
GGATGTAAACTGTTCTGATTTTTGGTGGCTGCATGCATTAACAATCTTTTTGTTGCATCCCTAGTTAATGACCTATCTGAGAACACCGTCCTGAGCGAATCCGAGTTTGAGCTACTAGACAACATCCTGCAGAACTCATTTCCCTCCATGCATGGACCAGGCCTGGGGCCTCTGCTGGAAACTGTGGTGGTCCAGTCTACAATTCCAACAGGTGAGCCGCAAATCCCACTCAAGACAAAAAACCCCCAGAGAGCAGGTCTATCCCTACTGGGAGTAACATTTAAAATTGTTTGTTGCAGACAATTCAGACGCCAAATACAGCTACTTCGATGAGTACACCAGCCAGCTGACCCCAGAGAGTGACCACGGCTACGACTCTCTCACGGAGAGCTTTCAGAGTTCCCATGCTGGTAAGAATCCCCACTAAAACCTAAACAACTCAGGTCAAGGGCGCTCTGTGAACGAACATTATTGAACATGTACTTCGGTTTGTCCTGTGT[A/C]GGCAGCTTCCTGAACCCGAGCTCACCTGAGTCCAACAGCAGTGATTCTGACCCTGAATACTCGGAGACTCCTTACTCCATCAGCTCCAGTAAGTTCCTCTCACTCGTCTACAGTTGCTCCACCTCACTCCTGCATGGCGATCTACCTGCAGAGTTTCACCTGAATAGGCCGACATGTGTCGTCAGGACTACCTGACAATCACACAGGCTGAAACTAAACTCTGCAGGAAGATGCTCCTCGAGTATACTGCCCTACAGAGGACAGTATCTACGCAAACACAAAGCTTTGACAACAGATCAGATTCTGTAGTTAATATACGTAGATTTACACCTCAATATTGACCAAATGTGTAGATACTGCTCCTTTTAGGGCAGCATAATAATAAGGGAGTTCCCTGGATGACCCCAAAACACAAACCTCTGACATTCAGTTGTATTGTCTGCTTTCCACAGAGAACTTTTCAAAACAAGAGCCAGAAAAGACCAAGAGAGGCAGAGGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25170
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113795 | Nonsense | 338 | 375 | 7 | 8 |
Genomic Location (Zv9):
Chromosome 22 (position 639292)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 626400 |
GRCz11 | 22 | 664123 |
KASP Assay ID:
554-7327.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGGGGGCAGAAGAAGAAGAACAGCAGCATGACCTACGAGAAGCTCAGC[A/T]GAGCCATGAGGTATAAATCAATCCTAAAATCACTGGGGAGCCTGGGAGCA
Long Flanking Sequence:
TATTGACCAAATGTGTAGATACTGCTCCTTTTAGGGCAGCATAATAATAAGGGAGTTCCCTGGATGACCCCAAAACACAAACCTCTGACATTCAGTTGTATTGTCTGCTTTCCACAGAGAACTTTTCAAAACAAGAGCCAGAAAAGACCAAGAGAGGCAGAGGACGACCTCCCAAGCTCAGGGATAGTGACGGATTTGATCACTTCATTCAGTCCAAGAAAAGCAAACATGGTGAGTACGCAGAGCTCTGCCTTTAGAGGCTCCTGATGCACACATATGCAGTGTACTAAACTAGACTCCACTGTTCCCCCAAAGCTCCAAGAGGAACCCACCTGTGGGAGTTCATCCGGGATATCCTGATCCACCCGGAGCAGAACCAGGGGCTGATGAAGTGGGAGGACCGCAGGGACGGCGTCTTCAAGTTCTTGAAGTCTGAAGCTGTTGCTCAGCTCTGGGGGCAGAAGAAGAAGAACAGCAGCATGACCTACGAGAAGCTCAGC[A/T]GAGCCATGAGGTATAAATCAATCCTAAAATCACTGGGGAGCCTGGGAGCAATAGGGGAGTCTGGGTTTGTGGCAGTGGAGCCTGGGACAGAAGAATAATCAAAACTCTTGCTCTTTCTGACAGGTATTACTACAAGAGAGAGATTCTGGAGAGGGTGGACGGACGGAGGCTTGTTTACAAGTTCGGGAAGAACTCCACCGGTTGGAGGATAGAGGAGACCGGTTATTAAAGTTGACCGTCGGAGATCGCTTTCAGGAAAAATGTAGAGACTTTGGACTCCTGCTAATGAGGAACTTTAAGCTAAGCTTGGATGCTCTGAAGATCCTCCCTTTAGAAACGCTCTCTTCCCAGAGGGAAAAGGTTTCACAGAAACTGTAAGCCAGTGTTTTGGCTAAAGTAGGTTTTATGAACCGGTAAACAGTGGCGATTGTCTGGTTGTAAGGGCACGCAGGCGTAGCCTGGTCCAGATATTGCTACACCACTAAAAGAGTCTAAGTCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24046
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113795 | Essential Splice Site | 341 | 375 | 7 | 8 |
Genomic Location (Zv9):
Chromosome 22 (position 639304)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 626412 |
GRCz11 | 22 | 664135 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAAGAAGAACAGCAGCATGACCTACGAGAAGCTCAGCAGAGCCATGAGG[T/C]ATAAATCAATCCTAAAATCACTGGGGAGCCTGGGAGCAATAGGGGAGTCT
Long Flanking Sequence:
GTGTAGATACTGCTCCTTTTAGGGCAGCATAATAATAAGGGAGTTCCCTGGATGACCCCAAAACACAAACCTCTGACATTCAGTTGTATTGTCTGCTTTCCACAGAGAACTTTTCAAAACAAGAGCCAGAAAAGACCAAGAGAGGCAGAGGACGACCTCCCAAGCTCAGGGATAGTGACGGATTTGATCACTTCATTCAGTCCAAGAAAAGCAAACATGGTGAGTACGCAGAGCTCTGCCTTTAGAGGCTCCTGATGCACACATATGCAGTGTACTAAACTAGACTCCACTGTTCCCCCAAAGCTCCAAGAGGAACCCACCTGTGGGAGTTCATCCGGGATATCCTGATCCACCCGGAGCAGAACCAGGGGCTGATGAAGTGGGAGGACCGCAGGGACGGCGTCTTCAAGTTCTTGAAGTCTGAAGCTGTTGCTCAGCTCTGGGGGCAGAAGAAGAAGAACAGCAGCATGACCTACGAGAAGCTCAGCAGAGCCATGAGG[T/C]ATAAATCAATCCTAAAATCACTGGGGAGCCTGGGAGCAATAGGGGAGTCTGGGTTTGTGGCAGTGGAGCCTGGGACAGAAGAATAATCAAAACTCTTGCTCTTTCTGACAGGTATTACTACAAGAGAGAGATTCTGGAGAGGGTGGACGGACGGAGGCTTGTTTACAAGTTCGGGAAGAACTCCACCGGTTGGAGGATAGAGGAGACCGGTTATTAAAGTTGACCGTCGGAGATCGCTTTCAGGAAAAATGTAGAGACTTTGGACTCCTGCTAATGAGGAACTTTAAGCTAAGCTTGGATGCTCTGAAGATCCTCCCTTTAGAAACGCTCTCTTCCCAGAGGGAAAAGGTTTCACAGAAACTGTAAGCCAGTGTTTTGGCTAAAGTAGGTTTTATGAACCGGTAAACAGTGGCGATTGTCTGGTTGTAAGGGCACGCAGGCGTAGCCTGGTCCAGATATTGCTACACCACTAAAAGAGTCTAAGTCAGAGATGTCAAACT
Associated Phenotype:
Not determined